GUDIDData
eudamed_udi Primary ID: 07312056570905

Formaldehyde 4% Q Path / FORMALINE 10% (UDI 07312056570905)

Manufactured by VWR INTERNATIONAL SAS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Formaldehyde 4% Q Path / FORMALINE 10% - Primary ID 07312056570905

Device Regulatory Overview

The Formaldehyde 4% Q Path / FORMALINE 10% (Model/Catalog Number: FOR0061A440396) is a medical device manufactured by VWR INTERNATIONAL SAS. This product is indexed under FDA Product Code / Category Classification W01030705 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FOR0061A440396
Product Code / EMDN
W01030705
Device Name
Q Path Fixative Formaldehyde
Database Sync Date
2026-08-09 16:50:43

Full Regulatory Attributes

πŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Formaldehyde 4% Q Path / FORMALINE 10%?

The registered manufacturer of record for Formaldehyde 4% Q Path / FORMALINE 10% is VWR INTERNATIONAL SAS.

What is the Primary UDI-DI identifier for Formaldehyde 4% Q Path / FORMALINE 10%?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056570905.

What classification code is assigned to this device?

This device is registered under product classification code W01030705.

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